Difference between revisions of "Part:BBa K3394000"
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− | We | + | We learned about the cellulase from a past iGEM team – the British Columbia 2016 team which fused it to the surface layer of Caulobacter crescentus (BBa_K2139001). In our project, we optimized the sequence for use in Escherichia coli, and it was synthesized by IDT for us. |
Furthermore, Endo5a was expressed with an N-terminal histidine tag (6-histidine tag) instead of the 17 first amino acids that served as a signal peptide (51 nucleotides). | Furthermore, Endo5a was expressed with an N-terminal histidine tag (6-histidine tag) instead of the 17 first amino acids that served as a signal peptide (51 nucleotides). | ||
Revision as of 14:46, 17 October 2020
Coding Sequence of Endo5a cellulase (for E. coli)
This part consists the coding region of Endo5A, an endo-1,4-beta-glucanase. Endo5a breaks down cellulose by cutting internal 1-4 beta glucose linkages in the cellulose chain.
The complete cellulose hydrolysis reaction involves this enzyme along with several other enzymes: endo-1,4-beta-glucanases, exo-1,4-beta-glucanases (or cellobiohydrolases) and beta-glucosidases.
Endo5a is a relatively small protein with an optimal temperature of 50 Celsius degrees and an optimal pH range of 6-7.
The NCBI Genbank number for Endo5a is HQ657203.1 (DNA), AEB00655.1 (amino acid).
We learned about the cellulase from a past iGEM team – the British Columbia 2016 team which fused it to the surface layer of Caulobacter crescentus (BBa_K2139001). In our project, we optimized the sequence for use in Escherichia coli, and it was synthesized by IDT for us.
Furthermore, Endo5a was expressed with an N-terminal histidine tag (6-histidine tag) instead of the 17 first amino acids that served as a signal peptide (51 nucleotides).
Endo5A was isolated from the bacterial flora found in the gut of a cotton bollworm (Helicoverpa armigera) which secretes a variety of plant-hydrolyzing enzymes.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 898
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 898
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 898
- 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 898
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 898
- 1000COMPATIBLE WITH RFC[1000]